Fidler Samantha J
Department of Clinical Immunology, PathWest Laboratory Medicine, Royal Perth Hospital, Perth, WA, Australia.
Methods Mol Biol. 2012;882:359-77. doi: 10.1007/978-1-61779-842-9_21.
The presence of preformed donor-specific HLA antibodies detected by Complement-dependent cyto-toxicity (CDC) crossmatch assay is associated with a high incidence of hyperacute or accelerated rejection and remains one of the gold standard tests pre-transplant. The standard CDC crossmatch detects IgG1, IgG3, and IgM antibody, i.e. complement fixing, bound to the native viable cell surface of lymphocytes. The crossmatch can be enhanced with the addition of anti-human-globulin to detect non-complement fixing antibodies (IgG2 and IgG4), and sensitivity can be improved with prolonged incubation times.
通过补体依赖细胞毒性(CDC)交叉配型试验检测到预先形成的供者特异性HLA抗体与超急性或加速性排斥反应的高发生率相关,并且仍然是移植前的金标准检测之一。标准的CDC交叉配型检测与淋巴细胞天然活细胞表面结合的IgG1、IgG3和IgM抗体,即补体结合抗体。通过添加抗人球蛋白来检测非补体结合抗体(IgG2和IgG4)可以增强交叉配型,延长孵育时间可以提高灵敏度。